US4983707A - Copolyester from 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate - Google Patents
Copolyester from 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate Download PDFInfo
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- US4983707A US4983707A US07/473,153 US47315390A US4983707A US 4983707 A US4983707 A US 4983707A US 47315390 A US47315390 A US 47315390A US 4983707 A US4983707 A US 4983707A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/60—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from the reaction of a mixture of hydroxy carboxylic acids, polycarboxylic acids and polyhydroxy compounds
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- This invention relates to a novel copolyester which is melt-processable at a temperature below about 400° C. and which can give molded articles having excellent heat resistance and hydrolysis resistance.
- Aromatic polyesters such as polyethylene terephthalate, polybutylene terephthalate, etc., have high crystallizability and high softening point, and are excellent in view of mechanical strength, etc., and they have therefore been widely used in fibers, films, and other molded articles. However, they are not necessarily satisfactory concerning heat resistance.
- thermotropic liquid crystal polyesters which exhibit optical anisotropy in a melt phase, attract attention from the viewpoint of excellent properties thereof.
- thermotropic liquid crystal polyesters Differing, to a great extent from conventional polyesters used widely in industry such as polyethylene terephthalate, polybutylene terephthalate, etc., the thermotropic liquid crystal polyesters have a molecular chain which does not bend easily even in a melt phase, or maintain a rod-like form. And when they are melted, the molecules are not much tangled one with another, and they exhibit a specific flow behavior of unidirectional orientation under a small shear stress, and even when they are cooled in the oriented state, they are solidified with maintaining the molecules in the oriented state. Thus, the thermotropic liquid crystal polyesters have excellent melt-processability, mechanical properties and heat resistance.
- thermotropic liquid crystal polyester As a thermotropic liquid crystal polyester, there is known a wholly aromatic polyester derived from p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid as main components, as is described in U.S. Pat. No. 4,161,470. This wholly aromatic polyester has excellent mechanical properties and heat resistance. Since, however, the 6-hydroxy-2-napthoic acid as the component is expensive and the resulting polymer is hence expensive, the expansion of use thereof is being prevented.
- a copolyester obtained by the polycondensation of polyethylene terephthalate under acidolysis with p-acetoxybenzoic acid is also known as a thermotropic liquid crystal, which can be melt-molded by using an ordinary injection molding machine used for molding polyethylene terephthalate, polybutylene terephthalate due to its low melt-processing temperature of about 240°-260° C., and which is relatively less expensive.
- this copolyester is not satisfactory in view of heat resistance since its heat distortion temperature is about 65°-70° C., and it also has another defect in that its hydrolysis resistance is inferior to those of wholly aromatic polyesters.
- thermotropic liquid crystal polyester excellent in melt-processability.
- thermotropic liquid crystal polyester excellent in mechanical properties.
- thermotropic liquid crystal polyester excellent in heat resistance and hydrolysis resistance.
- thermotropic liquid crystal polyester which is excellent in economy.
- melt-processable copolyester comprising:
- Y is at least one member selected from the group consisting of ##STR7## and a structural unit (IV) of the following formula (4)
- Z represents at least one member selected from the group consisting of ##STR8## the ratio of the structural unit (IV) to the structural units [(I)+(II)+(III)+(IV)] in total being 5 to 80 mole %, the structural units [(I)+(II)] being substantially equimolar to the structural unit (III), the ratio of the structural unit (I) to the structural units [(I)+(II)] in total being 10 to 90 mole %, and the copolyester having an inherent viscosity (ln ⁇ rel )/C, measured in a concentration of 0.16 g/dl in pentafluorophenol at 60° C., of not less than 0.3 dl/g.
- the formula (1) for the structural unit (I) represents a moiety of 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid.
- methyl p-hydroxybenzoate or ethyl p-hydroxybenzoate and 1,6-hexane dichloride or 1,6-hexane dibromide are reacted in an aprotic polar solvent, such as dimethylformamide, in the presence of an alkali, such as sodium carbonate to form dimethyl 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate or diethyl 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate.
- the above products are saponified with an alkali, e.g. potassium hydroxide, and further neutralized with hydrochloric acid, etc., whereby 1,6-bis(phenoxy)-hexane-4,4'-dicarboxylic acid is obtained.
- the formula (2) for the structural unit (II) represents a moiety of terephthalic acid, 4,4'-biphenyldicarboxylic acid or 2,6-naphthalenedicarboxylic acid, and the structural unit (II) may be formed of one moiety of these or two or more moieties of these in combination.
- the formula (3) for the structural unit (III) represents a moiety of 1,4-dihydroxybenzene, 1,3-dihydroxybenzene, 4,4'-dihydroxybiphenyl, 4,4'-dihydroxydiphenyl ether, or 4,4'-dihydroxybenzophenone, and the structural unit (III) may be formed of one moiety of these or two or more moieties of these in combination.
- the formula (4) for the structural unit (IV) represents a moiety of p-hydroxybenzoic acid or 6-hydroxy-2-naphthoic acid, and the structural unit (IV) may be formed of one moiety of these or more moieties in combination.
- the ratio of the structural unit (IV) to the structural units [(I)+(II)+(III)+(IV)] in total is 5 to 80 mole %, preferably 10 to 70 mole %, more preferably 40 to 70 mole %, and the ratio of the structural unit (I) to the structural units [(I)+(II)] in total is 10 to 90 mole %, preferably 15 to 85 mole %.
- the copolyester of this invention is melt-processable at temperature below 400° C., and makes it possible to easily obtain molded articles having excellent mechanical properties, heat resistance and hydrolysis resistance.
- the copolyester of this invention has an inherent viscosity (In ⁇ rel )/C, measured in a concentration of 0.16 g/dl in pentafluorophenol at 60° C., of not less than 0.3 dl/g, preferably 0.5 to 8.0 dl/g.
- the copolyester of this invention having an inherent viscosity within this range has both excellent mechanical strength and excellent melt-processability.
- the copolyester of this invention not only has better heat resistance and hydrolysis resistance than usual aromatic polyesters such as polyethylene terephthalate, etc., but also has better heat resistance and hydrolysis resistance than that liquid crystal polyester of U.S. Pat. No. 3,778,410 which is formed from polyethylene terephthalate and p-acetoxybenzoic acid. Further, the copolyester of this invention is less expensive than that liquid crystal wholly aromatic polyester of U.S. Pat. No. 4,161,470 which is formed from p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid.
- the copolyester of this invention can be produced according to a conventional polycondensation process used for producing usual polyesters. For example, it can be produced by reacting a 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid or its ester which forms a moiety of the formula (1) for the structural unit (I), an aromatic dicarboxylic acid or its ester which forms a moiety of the formula (2) for the structural unit (II), an aromatic dihydroxy compound or its ester which forms a moiety of the formula (3) for the structural unit (III) and an aromatic hydroxycarboxylic acid or its ester which forms a moiety of the formula (4) for the structural unit (IV), thereby to form ester bonds in such a manner that the ratio of the unit (IV) to the units [(I)+(II)+(III)+(IV)] in total, the ratio between the units (I) and (II), and the ratio of the unit (III) to the units [(I)+(II)]
- the process (a) is more desirable than the process (b) in that the polycondensation proceeds without any catalyst.
- the above process (b), however, can be carried out by using metal compounds such as stannous acetate, tetrabutyl-titanate, etc., as a catalyst for the polycondensation.
- the copolyester obtained by this invention is meltprocessable at temperature below 400° C., is capable of giving molded articles having excellent mechanical properties and resistance to heat and hydrolysis, and is industrially better than conventional thermotropic liquid crystal polyesters, e.g., those described in U.S. Pat. Nos. 4,161,470 and 3,778,410.
- the copolyester of this invention may contain a filler, stabilizer, glass fiber, fire retardant and other additives.
- a copolyester was dissolved in pentafluorophenol such that the copolyester cocentration was 0.16 g/dl, and the solution was subjected to an Ubbelode capillary viscometer (in which the flow time of pentafluorophenol alone was 286 seconds) at 60° ⁇ 0.01° C.
- a copolyester was dissolved in phenol/tetrachloroethane mixed solvents (the weight ratio of phenol/tetrachloroethane was 60/40) such that the copolyester concentrations were 0.50 g/dl, 0.25 g/dl and 0.17 g/dl, and the solutions were subjected to an Ubbelode capillary viscometer (in which the flow time of said mixed solvent alone was 140 seconds) at 25° ⁇ 0.01° C.
- the starting temperature of thermal decomposition was measured by subjecting 4 mg of a sample to measurement using a thermal analyzer (model TG/DTA 200 manufactured by Seiko Electronics) in which dry air was under circulation (flow rate: 300 ml/min) and the temperature elevation rate was 10° C./min.
- This temperature was measured by subjecting 10 mg of a sample contained in a non-closed aluminum container to measurement using a differential scanning calorimeter (DSC, model: SSC/560S, manufactured by Seiko Electronics) in which nitrogen gas was under circulation (flow rate: 30 ml/min) and the temperature elevation rate was 20° C./min.
- DSC differential scanning calorimeter
- the apparent melt viscosity was measured by using a flow tester (model: CFT-500 made by Shimadzu Corporation), which had a die having a diameter of 1 mm and a length of 2 mm.
- the load was 10 kg or 50 kg.
- a 1-liter autoclave having a stirrer, thermometer, pressure gauge and nitrogen gas-introducing tube was charged with 91.2 g of methyl p-hydroxybenzoate, 46.6 g of 1,6-hexane dichloride, 600 ml of dimethylformamide and 34.9 g of sodium carbonate, and closed.
- the stirring of the mixture and temperature elevation were started, and the reaction was carried out at 120° C. for 7 hours. Thereafter, the temperature was elevated to 130° C. to continue the reaction for 7 hours, during which the autoclave had an internal pressure of 5 kg/cm 2 .
- the reaction liquid was cooled, a precipitate was filtered and a separated crude dimethyl 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate was washed with water, and then with methanol to give 85.6 g of white plate-like crystals.
- 50 g of the white plate-like crystals were charged into a glass separable flask with a stirrer, thermometer and nitrogen gas-introducing tube, and 900 ml of ethyl alcohol and 52 g of sodium hydroxide were added.
- the mixture was heat-treated at 80° C. for 4 hours to saponify the dimethyl 1,6-bis(phenoxy)-hexane-4,4'-dicarboxylate.
- This treated liquid was neutralized by adding 2,000 ml of water and 100 ml of 35% hydrochloric acid to give a crude 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid.
- This product was washed with water and filtered repeatedly to give 37 g of a high-purity 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid (to be referred to as "BHB" hereinbelow).
- a 50-milliliter reactor having a stirrer, thermometer, pressure gauge, nitrogen gas-introducing tube and a distillation head connected to a condenser was charged with 10.8 g (0.06 mole) of p-acetoxybenzoic acid, 3.88 g (0.02 mole) of hydroquinone diacetate, 5.38 g (0.015 mole) of "BHB" and 0.83 g (0.005 mole) of terephthalic acid, and a purge with nitrogen was carried out 3 times. Then, the mixture was heated up to 200° C. while a small amount of nitrogen was introduced into the reactor with stirring the mixture moderately.
- the stirring rate was increased, and the temperature of the mixture was increased stepwise to carry out a reaction at 240° C. for 2 hours, at 260° C. for 2 hours, at 280° C. for 2 hours, at 300° C. for 1 hour, 320° C. for 1.5 hours and at 350° C. for 4 hours.
- the amount of acetic acid which had been distilled off was 4.9 g.
- the pressure of the reaction vessel was gradually reduced, and while the pressure was maintained at a vacuum of 0.5 Torr, the reaction product was stirred at 350° C. for 4 hours to complete the polymerization, whereby a polymer (to be referred to as "A-1" hereinbelow) was obtained.
- the polymer "A-1” had an inherent viscosity of 1.92. When this polymer was subjected to a differential scanning calorimeter (DSC), no clear endotherm was observed. This polymer exhibited optical anisotropy in a molten state.
- DSC differential scanning calorimeter
- Example 2 The same reactor as that used in Example 1 was charged with 10.8 g (0.06 mol) of p-acetoxybenzoic acid, 5.41 g (0.02 mole) of 4,4'-diacetoxybiphenyl, 3.58 g (0.01 mole) of "BHB" and 1.66 g (0.01 mole) of terephthalic acid, and the procedure of Example 1 was repeated to carry out a reaction at 240° C. for 3 hours, at 250° C. for 3 hours, and at 280° C. for 4.5 hours. The amount of acetic acid which had been distilled off was 3.9 g.
- the polymer "A-2” had an inherent viscosity of 4.62. When this polymer was subjected to a differential scanning calorimeter (DSC), an endotherm at 314° C. was observed.
- DSC differential scanning calorimeter
- Example 2 was repeated except for the use, in place of 5.41 g (0.02 mol) of the 4,4'-diacetoxybiphenyl, of 5.73 g (0.02 mole) of 4,4'-diacetoxydiphenyl ether (Example 3), 5.97 g (0.02 mole) of 4,4'-diacetoxybenzophenone (Example 4) and 3.88 g (0.02 mole) of resorcinol diacetate (Example 5), whereby polymers "A-3" to "A-5" were obtained.
- Table 1 shows their inherent viscosities, DSC-measured temperatures indicating endotherm caused by melting thereof (Tm), and starting temperatures of thermal decomposition (Td).
- Example 2 The same reactor as that used in Example 1 was charged with 7.56 g (0.042 mol) of p-acetoxybenzoic acid, 4.14 g (0.018 mole) of 6-acetoxy-2-naphthoic acid, 3.88 g (0.02 mole) of hydroquinone diacetate, 3.58 g (0.01 mole) of "BHB” and 1.66 g (0.01 mole) of terephthalic acid, and the procedure of Example 1 was repeated to carry out a reaction at 240° C. for 2 hours and at 260° C. for 3.5 hours. The amount of acetic acid which had been distilled off was 4.9 g.
- the polymer "A-2” had an inherent viscosity of 1.65. When this polymer was subjected to a differential scanning calorimeter (DSC), an endotherm at 275° C. was observed. This polymer exhibited optical anisotropy in a molten state.
- DSC differential scanning calorimeter
- Example 6 was repeated except for the use, in place of 3.88 g (0.02 mol) of the hydroquinone diacetate, of 5.73 g (0.02 mole) of 4,4'-diacetoxydiphenyl ether (Example 7) and 5.97 g (0.02 mole) of 4,4'-diacetoxybenzophenone (Example 8), whereby polymers "A-7" to "A-8" were obtained.
- Table 1 shows their inherent viscosities, DSC-measured temperatures indicating endotherm caused by melting thereof (Tm) and starting temperatures of thermal decomposition (Td).
- Example 2 The same reactor as that used in Example 1 was charged with 10.8 g (0.06 mol) of p-acetoxybenzoic acid, 3.88 g (0.02 mole) of hydroquinone diacetate, 3.58 g (0.01 mole) of "BHB" and 2.16 g (0.01 mole) of 2,6-naphthalenedicarboxylic acid, and the procedure of Example 1 was repeated to carry out a reaction at 240° C. for 3.5 hours, at 260° C. for 2 hours and at 280° C. for 1.5 hours. The amount of acetic acid which had been distilled off was 4.8 g.
- the polymer "B-1" had an inherent viscosity of 2.56. When this polymer was subjected to a differential scanning calorimeter (DSC), an endotherm at 286° C. was observed. This polymer exhibited optical anisotropy in a molten state.
- DSC differential scanning calorimeter
- Example 2 The same reactor as that used in Example 1 was charged with 10.8 g (0.06 mol) of p-acetoxybenzoic acid, 3.88 g (0.02 mole) of hydroquinone diacetate, 3.58 g (0.01 mole) of "BHB" and 2.42 g (0.01 mole) of 4,4'-biphenyldicarboxylic acid, and the procedure of Example 1 was repeated to carry out a reaction at 240° C. for 2 hours, at 260° C. for 2 hours, at 280° C. for 2 hours, at 300° C. for 1 hour and at 320° C. for 3 hours. The amount of acetic acid which had been distilled off was 4.9 g.
- the polymer "B-2” had an inherent viscosity of 3.07. When this polymer was subjected to a differential scanning calorimeter (DSC), an endotherm at 355° C. was observed. This polymer exhibited optical anisotropy in a molten state.
- DSC differential scanning calorimeter
- Example 10 was repeated except for the use, in place of 3.88 g (0.02 mol) of the hydroquinone diacetate, of 5.41 g (0.02 mole) of 4,4'-diacetoxybiphenyl (Example 11), 5.73 g (0.02 mole) of 4,4'-diacetoxydiphenyl ether (Example 12), 5.97 g (0.02 mole) of 4,4'-diacetoxybenzophenone (Example 13) and 3.88 g (0.02 mole) of resorcinol diacetate (Example 14), whereby polymers "B-3" to "B-6" were obtained.
- Table 2 shows their inherent viscosities, DSC-measured temperatures indicating endotherm caused by melting thereof (Tm) and starting temperatures of thermal decomposition (Td).
- Table 3 shows elemental analysis values of the polymers obtained in Examples 1 to 14. The values in "O(%)" in Table 3 were calculated by deducting values for C(%) and H(%) from 100%.
- Table 4 shows apparent melt-viscosities of the polymers obtained in Examples 1 to 14.
- the mixture was heated while it was stirred, and when the temperature reached 280° C., the pressure was reduced gradually to 0.5 Torr for about 30 minutes. While the vacuum degree was maintained at not more than 0.5 Torr, a polycondensation reaction was carried out, and when a prescribed torque was reached, the reaction was stopped, whereby a polyethylene terephthalate "C-1" was obtained.
- the polyethylene terephthalate C-1 had an intrinsic viscosity of 0.62 and a terminal carboxyl group concentration of 18.7 eq/10 6 g.
- Table 1 also shows its Td and DSC-measured temperature (Tm) indicating endotherm caused by melting thereof.
- Table 1 shows its Td and DSC-measured temperature (Tm) indicating heat absorption caused by melting thereof.
Abstract
A melt-processable copolyester comprising:
a structural unit (I) of the formula (1), ##STR1## a structural unit (II) of the formula (2),
--OC--X--CO-- (2)
wherein X is at least one member selected from the group consisting of ##STR2## a structural unit (III) of the formula (3)
--O--Y--O-- (3)
wherein Y is at least one member selected from the group consisting of ##STR3## and a structural unit (IV) of the formula (4)
--O--Z--CO-- (4)
wherein Z represents at least one member selected from the group consisting of ##STR4## the ratio of the structural unit (IV) (III) to the structural units [(I)+(II)+(III)+(IV)] in total being 5 to 80 mole%, the structural units [(I)+(II)] being substantially equimolar to the structural unit (III), the ratio of the structural unit (I) to the structural units [(I)+(II)] in total being 10 to 90 mole %, and the copolyester having an inherent viscosity (ln ηrel)/C, measured in a concentration of 0.16 g/dl in pentafluorophenol at 60° C., of not less than 0.3 dl/g.
Description
This invention relates to a novel copolyester which is melt-processable at a temperature below about 400° C. and which can give molded articles having excellent heat resistance and hydrolysis resistance.
Aromatic polyesters such as polyethylene terephthalate, polybutylene terephthalate, etc., have high crystallizability and high softening point, and are excellent in view of mechanical strength, etc., and they have therefore been widely used in fibers, films, and other molded articles. However, they are not necessarily satisfactory concerning heat resistance.
With recent advancing technologies, there is an increasing demand for materials having higher performance, and a variety of polyesters having various novel performances have been developed and are already commercially available.
Above all, thermotropic liquid crystal polyesters, which exhibit optical anisotropy in a melt phase, attract attention from the viewpoint of excellent properties thereof.
Differing, to a great extent from conventional polyesters used widely in industry such as polyethylene terephthalate, polybutylene terephthalate, etc., the thermotropic liquid crystal polyesters have a molecular chain which does not bend easily even in a melt phase, or maintain a rod-like form. And when they are melted, the molecules are not much tangled one with another, and they exhibit a specific flow behavior of unidirectional orientation under a small shear stress, and even when they are cooled in the oriented state, they are solidified with maintaining the molecules in the oriented state. Thus, the thermotropic liquid crystal polyesters have excellent melt-processability, mechanical properties and heat resistance.
As a thermotropic liquid crystal polyester, there is known a wholly aromatic polyester derived from p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid as main components, as is described in U.S. Pat. No. 4,161,470. This wholly aromatic polyester has excellent mechanical properties and heat resistance. Since, however, the 6-hydroxy-2-napthoic acid as the component is expensive and the resulting polymer is hence expensive, the expansion of use thereof is being prevented.
On the other hand, as shown in U.S. Pat. No. 3,778,410, a copolyester obtained by the polycondensation of polyethylene terephthalate under acidolysis with p-acetoxybenzoic acid is also known as a thermotropic liquid crystal, which can be melt-molded by using an ordinary injection molding machine used for molding polyethylene terephthalate, polybutylene terephthalate due to its low melt-processing temperature of about 240°-260° C., and which is relatively less expensive. However, this copolyester is not satisfactory in view of heat resistance since its heat distortion temperature is about 65°-70° C., and it also has another defect in that its hydrolysis resistance is inferior to those of wholly aromatic polyesters.
It is an object of this invention to provide a thermotropic liquid crystal polyester excellent in melt-processability.
It is another object of this invention to provide a thermotropic liquid crystal polyester excellent in mechanical properties.
Further, it is another object of this invention to provide a thermotropic liquid crystal polyester excellent in heat resistance and hydrolysis resistance.
It is yet another object of this invention to provide a thermotropic liquid crystal polyester which is excellent in economy.
According to this invention, there is provided a melt-processable copolyester comprising:
a structural unit (I) of the following formula (1), ##STR5## a structural unit (II) of the following formula (2),
--OC--X--CO-- (2)
wherein X is at least one member selected from the group consisting of ##STR6## a structural unit (III) of the following formula (3)
--O--Y--O-- (3)
wherein Y is at least one member selected from the group consisting of ##STR7## and a structural unit (IV) of the following formula (4)
--O--Z--CO-- (4)
wherein Z represents at least one member selected from the group consisting of ##STR8## the ratio of the structural unit (IV) to the structural units [(I)+(II)+(III)+(IV)] in total being 5 to 80 mole %, the structural units [(I)+(II)] being substantially equimolar to the structural unit (III), the ratio of the structural unit (I) to the structural units [(I)+(II)] in total being 10 to 90 mole %, and the copolyester having an inherent viscosity (ln ηrel)/C, measured in a concentration of 0.16 g/dl in pentafluorophenol at 60° C., of not less than 0.3 dl/g.
In the copolyester of this invention, the formula (1) for the structural unit (I) represents a moiety of 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid.
No special limitation is imposed on the process for the production of the 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid, and it may be produced, for example, by the following process.
First, methyl p-hydroxybenzoate or ethyl p-hydroxybenzoate and 1,6-hexane dichloride or 1,6-hexane dibromide are reacted in an aprotic polar solvent, such as dimethylformamide, in the presence of an alkali, such as sodium carbonate to form dimethyl 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate or diethyl 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate. Then, the above products are saponified with an alkali, e.g. potassium hydroxide, and further neutralized with hydrochloric acid, etc., whereby 1,6-bis(phenoxy)-hexane-4,4'-dicarboxylic acid is obtained.
The formula (2) for the structural unit (II) represents a moiety of terephthalic acid, 4,4'-biphenyldicarboxylic acid or 2,6-naphthalenedicarboxylic acid, and the structural unit (II) may be formed of one moiety of these or two or more moieties of these in combination.
The formula (3) for the structural unit (III) represents a moiety of 1,4-dihydroxybenzene, 1,3-dihydroxybenzene, 4,4'-dihydroxybiphenyl, 4,4'-dihydroxydiphenyl ether, or 4,4'-dihydroxybenzophenone, and the structural unit (III) may be formed of one moiety of these or two or more moieties of these in combination.
The formula (4) for the structural unit (IV) represents a moiety of p-hydroxybenzoic acid or 6-hydroxy-2-naphthoic acid, and the structural unit (IV) may be formed of one moiety of these or more moieties in combination.
In the copolyester of this invention, the ratio of the structural unit (IV) to the structural units [(I)+(II)+(III)+(IV)] in total is 5 to 80 mole %, preferably 10 to 70 mole %, more preferably 40 to 70 mole %, and the ratio of the structural unit (I) to the structural units [(I)+(II)] in total is 10 to 90 mole %, preferably 15 to 85 mole %.
The copolyester of this invention is melt-processable at temperature below 400° C., and makes it possible to easily obtain molded articles having excellent mechanical properties, heat resistance and hydrolysis resistance.
When the ratio of the structural unit (IV) to the structural units [(I)+(II)+(III)+(IV)] in total is lower than the above lower limit or higher than the above upper limit, resultant copolyesters have poor melt-processability, and the objects of this invention cannot be accomplished.
When the ratio of the structural unit (I) to the structural units [(I)+(II)] in total is lower than the above lower limit, resultant copolyesters have poor melt-processability, and the objects of this invention cannot be accomplished. When this ratio is higher than the above upper limit, resultant copolyesters have poor heat resistance, and the objects of this invention cannot be accomplished, either.
The copolyester of this invention has an inherent viscosity (In ηrel)/C, measured in a concentration of 0.16 g/dl in pentafluorophenol at 60° C., of not less than 0.3 dl/g, preferably 0.5 to 8.0 dl/g. The copolyester of this invention having an inherent viscosity within this range has both excellent mechanical strength and excellent melt-processability.
The copolyester of this invention not only has better heat resistance and hydrolysis resistance than usual aromatic polyesters such as polyethylene terephthalate, etc., but also has better heat resistance and hydrolysis resistance than that liquid crystal polyester of U.S. Pat. No. 3,778,410 which is formed from polyethylene terephthalate and p-acetoxybenzoic acid. Further, the copolyester of this invention is less expensive than that liquid crystal wholly aromatic polyester of U.S. Pat. No. 4,161,470 which is formed from p-hydroxybenzoic acid and 6-hydroxy-2-naphthoic acid.
The copolyester of this invention can be produced according to a conventional polycondensation process used for producing usual polyesters. For example, it can be produced by reacting a 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid or its ester which forms a moiety of the formula (1) for the structural unit (I), an aromatic dicarboxylic acid or its ester which forms a moiety of the formula (2) for the structural unit (II), an aromatic dihydroxy compound or its ester which forms a moiety of the formula (3) for the structural unit (III) and an aromatic hydroxycarboxylic acid or its ester which forms a moiety of the formula (4) for the structural unit (IV), thereby to form ester bonds in such a manner that the ratio of the unit (IV) to the units [(I)+(II)+(III)+(IV)] in total, the ratio between the units (I) and (II), and the ratio of the unit (III) to the units [(I)+(II)] in total come under the prescribed ranges. Typical examples of the production process include the following (a) and (b).
(a) Polycondensation of aromatic dicarboxylic acids, a diacetate of an aromatic dihydroxy compound and an acetate of an aromatic hydroxycarboxylic acid, during which acetic acids are removed. Examples of the polycondensation are: a reaction of 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid, terephthalic acid, 4,4'-diacetoxydiphenyl ether and p-acetoxybenzoic acid; a reaction of 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid, 2,6-naphthalenedicarboxylic acid, hydroquinone diacetate and p-acetoxybenzoic acid; a reaction of 1,6-bis(phenoxy)hexane-4,4-dicarboxylic acid, 4,4'-biphenyldicarboxylic acid, hydroquinone diacetate, p-acetoxybenzoic acid and 6-acetoxy-2-naphthoic acid; etc.
(b) Polycondensation of a diphenyl ester of aromatic dicarboxylic acids, an aromatic dihydroxy compound, a phenyl ester of an aromatic hydroxycarboxylic acid, during which phenols are removed. Examples of the polycondensation are: a reaction of diphenyl 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate, diphenyl terephthlate, 4,4'-dihydroxybenzophenone and phenyl p-hydroxy-benzoate; a reaction of diphenyl 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate, diphenyl 2,6-naphthalenedicarboxylate, hydroquinone and phenyl-p-hydroxybenzoate; a reaction of diphenyl 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate, diphenyl 4,4'-biphenyldicarboxylate, 4,4'-dihydroxybiphenyl, phenyl p-hydroxybenzoate and phenyl-6-hydroxy-2-naphthoate; etc.
Among these processes, the process (a) is more desirable than the process (b) in that the polycondensation proceeds without any catalyst. The above process (b), however, can be carried out by using metal compounds such as stannous acetate, tetrabutyl-titanate, etc., as a catalyst for the polycondensation.
The copolyester obtained by this invention is meltprocessable at temperature below 400° C., is capable of giving molded articles having excellent mechanical properties and resistance to heat and hydrolysis, and is industrially better than conventional thermotropic liquid crystal polyesters, e.g., those described in U.S. Pat. Nos. 4,161,470 and 3,778,410.
The copolyester of this invention may contain a filler, stabilizer, glass fiber, fire retardant and other additives.
This invention will be explained in detail according to Examples hereinbelow, which, however, shall not limit the present invention.
The physical properties, etc., set forth in Example and Comparative Examples were evaluated in the following methods.
(1) Inherent viscosity
A copolyester was dissolved in pentafluorophenol such that the copolyester cocentration was 0.16 g/dl, and the solution was subjected to an Ubbelode capillary viscometer (in which the flow time of pentafluorophenol alone was 286 seconds) at 60°±0.01° C.
On the basis of a flow time obtained by the above measurement, ηrel was determined, and the inherent viscosity [(Inηrel)/C] (dl/g) was calculated.
(2) Intrinsic viscosity
A copolyester was dissolved in phenol/tetrachloroethane mixed solvents (the weight ratio of phenol/tetrachloroethane was 60/40) such that the copolyester concentrations were 0.50 g/dl, 0.25 g/dl and 0.17 g/dl, and the solutions were subjected to an Ubbelode capillary viscometer (in which the flow time of said mixed solvent alone was 140 seconds) at 25°±0.01° C.
On the basis of flow times obtained by the above measurement, ηsp /C. was determined and extrapolated into a concentration of zero, and the intrinsic viscosity was determined.
(3) Starting temperature of thermal decomposition: Td (°C.)
The starting temperature of thermal decomposition was measured by subjecting 4 mg of a sample to measurement using a thermal analyzer (model TG/DTA 200 manufactured by Seiko Electronics) in which dry air was under circulation (flow rate: 300 ml/min) and the temperature elevation rate was 10° C./min.
(4) Temperature indicating endotherm caused by the melting of a polymer: Tm (°C.)
This temperature was measured by subjecting 10 mg of a sample contained in a non-closed aluminum container to measurement using a differential scanning calorimeter (DSC, model: SSC/560S, manufactured by Seiko Electronics) in which nitrogen gas was under circulation (flow rate: 30 ml/min) and the temperature elevation rate was 20° C./min.
(5) Apparent melt viscosity
The apparent melt viscosity was measured by using a flow tester (model: CFT-500 made by Shimadzu Corporation), which had a die having a diameter of 1 mm and a length of 2 mm. The load was 10 kg or 50 kg.
(6) Optical anisotropy
Whether or not a polymer had optical anisotropy was observed by using a polarizing microscope Optiphoto-POL (manufactured by Nikon) equipped with a hot stage (manufactured by Metler).
The following is a process employed to produce 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid used in the production of copolyesters in Examples.
A 1-liter autoclave having a stirrer, thermometer, pressure gauge and nitrogen gas-introducing tube was charged with 91.2 g of methyl p-hydroxybenzoate, 46.6 g of 1,6-hexane dichloride, 600 ml of dimethylformamide and 34.9 g of sodium carbonate, and closed. The stirring of the mixture and temperature elevation were started, and the reaction was carried out at 120° C. for 7 hours. Thereafter, the temperature was elevated to 130° C. to continue the reaction for 7 hours, during which the autoclave had an internal pressure of 5 kg/cm2.
The reaction liquid was cooled, a precipitate was filtered and a separated crude dimethyl 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate was washed with water, and then with methanol to give 85.6 g of white plate-like crystals. 50 g of the white plate-like crystals were charged into a glass separable flask with a stirrer, thermometer and nitrogen gas-introducing tube, and 900 ml of ethyl alcohol and 52 g of sodium hydroxide were added. The mixture was heat-treated at 80° C. for 4 hours to saponify the dimethyl 1,6-bis(phenoxy)-hexane-4,4'-dicarboxylate. This treated liquid was neutralized by adding 2,000 ml of water and 100 ml of 35% hydrochloric acid to give a crude 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid. This product was washed with water and filtered repeatedly to give 37 g of a high-purity 1,6-bis(phenoxy)hexane-4,4'-dicarboxylic acid (to be referred to as "BHB" hereinbelow).
A 50-milliliter reactor having a stirrer, thermometer, pressure gauge, nitrogen gas-introducing tube and a distillation head connected to a condenser was charged with 10.8 g (0.06 mole) of p-acetoxybenzoic acid, 3.88 g (0.02 mole) of hydroquinone diacetate, 5.38 g (0.015 mole) of "BHB" and 0.83 g (0.005 mole) of terephthalic acid, and a purge with nitrogen was carried out 3 times. Then, the mixture was heated up to 200° C. while a small amount of nitrogen was introduced into the reactor with stirring the mixture moderately. When the temperature of the mixture reached 200° C., the stirring rate was increased, and the temperature of the mixture was increased stepwise to carry out a reaction at 240° C. for 2 hours, at 260° C. for 2 hours, at 280° C. for 2 hours, at 300° C. for 1 hour, 320° C. for 1.5 hours and at 350° C. for 4 hours. The amount of acetic acid which had been distilled off was 4.9 g. Then, the pressure of the reaction vessel was gradually reduced, and while the pressure was maintained at a vacuum of 0.5 Torr, the reaction product was stirred at 350° C. for 4 hours to complete the polymerization, whereby a polymer (to be referred to as "A-1" hereinbelow) was obtained.
The polymer "A-1" had an inherent viscosity of 1.92. When this polymer was subjected to a differential scanning calorimeter (DSC), no clear endotherm was observed. This polymer exhibited optical anisotropy in a molten state.
The same reactor as that used in Example 1 was charged with 10.8 g (0.06 mol) of p-acetoxybenzoic acid, 5.41 g (0.02 mole) of 4,4'-diacetoxybiphenyl, 3.58 g (0.01 mole) of "BHB" and 1.66 g (0.01 mole) of terephthalic acid, and the procedure of Example 1 was repeated to carry out a reaction at 240° C. for 3 hours, at 250° C. for 3 hours, and at 280° C. for 4.5 hours. The amount of acetic acid which had been distilled off was 3.9 g. Then, the pressure of the reactor was gradually reduced, and while the pressure was maintained at a vacuum of 0.5 Torr, the reaction product was stirred at 280° C. for 3 hours, at 320° C. for 1 hour and at 350° C. for 1 hour to complete the polymerization, whereby a polymer (to be referred to as "A-2" hereinbelow) was obtained.
The polymer "A-2" had an inherent viscosity of 4.62. When this polymer was subjected to a differential scanning calorimeter (DSC), an endotherm at 314° C. was observed.
Example 2 was repeated except for the use, in place of 5.41 g (0.02 mol) of the 4,4'-diacetoxybiphenyl, of 5.73 g (0.02 mole) of 4,4'-diacetoxydiphenyl ether (Example 3), 5.97 g (0.02 mole) of 4,4'-diacetoxybenzophenone (Example 4) and 3.88 g (0.02 mole) of resorcinol diacetate (Example 5), whereby polymers "A-3" to "A-5" were obtained. Table 1 shows their inherent viscosities, DSC-measured temperatures indicating endotherm caused by melting thereof (Tm), and starting temperatures of thermal decomposition (Td).
The same reactor as that used in Example 1 was charged with 7.56 g (0.042 mol) of p-acetoxybenzoic acid, 4.14 g (0.018 mole) of 6-acetoxy-2-naphthoic acid, 3.88 g (0.02 mole) of hydroquinone diacetate, 3.58 g (0.01 mole) of "BHB" and 1.66 g (0.01 mole) of terephthalic acid, and the procedure of Example 1 was repeated to carry out a reaction at 240° C. for 2 hours and at 260° C. for 3.5 hours. The amount of acetic acid which had been distilled off was 4.9 g. Then, the pressure of the reactor was gradually reduced, and while the pressure was maintained at a vacuum of 0.5 Torr, the reaction product was stirred at 280° C. for 2 hours and at 300° C. for 3 hours to complete the polymerization, whereby a polymer (to be referred to as "A-6" hereinbelow) was obtained.
The polymer "A-2" had an inherent viscosity of 1.65. When this polymer was subjected to a differential scanning calorimeter (DSC), an endotherm at 275° C. was observed. This polymer exhibited optical anisotropy in a molten state.
Example 6 was repeated except for the use, in place of 3.88 g (0.02 mol) of the hydroquinone diacetate, of 5.73 g (0.02 mole) of 4,4'-diacetoxydiphenyl ether (Example 7) and 5.97 g (0.02 mole) of 4,4'-diacetoxybenzophenone (Example 8), whereby polymers "A-7" to "A-8" were obtained. Table 1 shows their inherent viscosities, DSC-measured temperatures indicating endotherm caused by melting thereof (Tm) and starting temperatures of thermal decomposition (Td).
The same reactor as that used in Example 1 was charged with 10.8 g (0.06 mol) of p-acetoxybenzoic acid, 3.88 g (0.02 mole) of hydroquinone diacetate, 3.58 g (0.01 mole) of "BHB" and 2.16 g (0.01 mole) of 2,6-naphthalenedicarboxylic acid, and the procedure of Example 1 was repeated to carry out a reaction at 240° C. for 3.5 hours, at 260° C. for 2 hours and at 280° C. for 1.5 hours. The amount of acetic acid which had been distilled off was 4.8 g. Then, the pressure of the reactor was gradually reduced, and while the pressure was maintained at a vacuum of 0.5 Torr, the reaction product was stirred at 280° C. for 3.5 hours and at 300° C. for 3 hours to complete the polymerization, whereby a polymer (to be referred to as "B-1" hereinbelow) was obtained.
The polymer "B-1" had an inherent viscosity of 2.56. When this polymer was subjected to a differential scanning calorimeter (DSC), an endotherm at 286° C. was observed. This polymer exhibited optical anisotropy in a molten state.
The same reactor as that used in Example 1 was charged with 10.8 g (0.06 mol) of p-acetoxybenzoic acid, 3.88 g (0.02 mole) of hydroquinone diacetate, 3.58 g (0.01 mole) of "BHB" and 2.42 g (0.01 mole) of 4,4'-biphenyldicarboxylic acid, and the procedure of Example 1 was repeated to carry out a reaction at 240° C. for 2 hours, at 260° C. for 2 hours, at 280° C. for 2 hours, at 300° C. for 1 hour and at 320° C. for 3 hours. The amount of acetic acid which had been distilled off was 4.9 g. Then, the pressure of the reactor was gradually reduced, and while the pressure was maintained at a vacuum of 0.5 Torr, the reaction product was stirred at 320° C. for 3 hours and at 330° C. for 3 hours to complete the polymerization, whereby a polymer (to be referred to as "B-2" hereinbelow) was obtained.
The polymer "B-2" had an inherent viscosity of 3.07. When this polymer was subjected to a differential scanning calorimeter (DSC), an endotherm at 355° C. was observed. This polymer exhibited optical anisotropy in a molten state.
Example 10 was repeated except for the use, in place of 3.88 g (0.02 mol) of the hydroquinone diacetate, of 5.41 g (0.02 mole) of 4,4'-diacetoxybiphenyl (Example 11), 5.73 g (0.02 mole) of 4,4'-diacetoxydiphenyl ether (Example 12), 5.97 g (0.02 mole) of 4,4'-diacetoxybenzophenone (Example 13) and 3.88 g (0.02 mole) of resorcinol diacetate (Example 14), whereby polymers "B-3" to "B-6" were obtained. Table 2 shows their inherent viscosities, DSC-measured temperatures indicating endotherm caused by melting thereof (Tm) and starting temperatures of thermal decomposition (Td).
Table 3 shows elemental analysis values of the polymers obtained in Examples 1 to 14. The values in "O(%)" in Table 3 were calculated by deducting values for C(%) and H(%) from 100%.
Table 4 shows apparent melt-viscosities of the polymers obtained in Examples 1 to 14.
A 5-liter autoclave having a stirrer, thermometer, pressure gauge, nitrogen gas-introducing tube, distillation head connected to a condenser, etc., was charged with 1,495 g (9.0 moles) of terephthalic acid and 838 g (13.5 moles) of ethylene glycol in this order, and the stirring of the mixture at a slow speed was started. After a purge with nitrogen was carried out three times, the internal pressure of the reactor was adjusted to 2 kg/cm2 with nitrogen, and while the mixture was stirred at 200 rpm, the heating of the mixture was started.
Care being taken not to allow the internal pressure to exceed 2.5 kg/cm2, a dehydration-condensation reaction was carried out between 215° C. and 240° C. to give an initial condensate. 1.3 g of triphenylphosphite and 0.4 g of germanium dioxide were added to the initial condensate, and the mixture was stirred for about 5 minutes and then transferred to a 5-liter condensation reactor.
The mixture was heated while it was stirred, and when the temperature reached 280° C., the pressure was reduced gradually to 0.5 Torr for about 30 minutes. While the vacuum degree was maintained at not more than 0.5 Torr, a polycondensation reaction was carried out, and when a prescribed torque was reached, the reaction was stopped, whereby a polyethylene terephthalate "C-1" was obtained. The polyethylene terephthalate C-1 had an intrinsic viscosity of 0.62 and a terminal carboxyl group concentration of 18.7 eq/106 g. Table 1 also shows its Td and DSC-measured temperature (Tm) indicating endotherm caused by melting thereof.
A 300-milliliter reactor having a stirrer, thermometer, pressure gauge, nitrogen gas-introducing tube, distillation head connected to a condenser, etc., was charged with 76.8 g of "C-1" and 108 g of p-acetoxybenzoic acid, and a purge with nitrogen was carried out three times.
While this mixture was stirred under a nitrogen atmosphere at 275° C., a reaction thereof was carried out to remove acetic acid. Then, the reaction mixture was subjected to a polycondensation reaction for 4 hours under a vacuum of not more than 0.5 Torr to give a polyester "C-2" having an intrinsic viscosity of 0.59 and a terminal carboxylic acid concentration of 149 eq/106 g. This polymer exhibited optical anisotropy in a molten state.
Table 1 shows its Td and DSC-measured temperature (Tm) indicating heat absorption caused by melting thereof.
Tables 1 and 2 clearly show that the polymers "A-1" to "A-8" and "B-1" to "B-8" had excellent heat resistance over the polymers "C-1" and "C-2".
TABLE 1
__________________________________________________________________________
Copolyester
Polyester Material formulation (molar ratio) *2
Tm Td
No.
BHB
TA HQDA
DABP
DADE
DABE
REDA
ABA
ANA (°C.)
(°C.)
__________________________________________________________________________
Inherent
Example Viscosity
1 A-1
15 5 20 60 1.92 *1
407
2 A-2
10 10 20 60 4.62 314
401
3 A-3
10 10 20 60 3.44 335
405
4 A-4
10 10 20 60 1.38 255
405
5 A-5
10 10 20 60 2.14 345
404
6 A-6
10 10 20 42 18 2.54 257
423
7 A-7
10 10 20 42 18 4.88 223
425
8 A-8
10 10 20 42 18 2.85 *1
402
Comparative (Intrinsic
Example viscosity)
1 C-1
Polyethylene terephthalate (0.62)
260
387
2 C-2
Polyethylene terephthalate/ABA = 40/60 (molar
(0.59)
200
397
__________________________________________________________________________
Note 1: *1 = Not detectable
Note 2: *2
BHB: 1,6bis(phenoxy)hexane-4,4dicarboxylic acid
TA: terephthalic acid
HQDA: hydroquinone diacetate
DABP: 4,4diacetoxybiphenyl
DADE: 4,4diacetoxydiphenyl ether
DABE: 4,4diacetoxybenzophenone
REDA: resorcinol diacetate
ABA: pacetoxybenzoic acid
ANA: 6acetoxy-2-naphthoic acid
Tm: DSCmeasured temperature indicating endotherm caused by melting of a
polymer
Td: Starting temperature of thermal decomposition
TABLE 2
__________________________________________________________________________
Copolyester
Polyester Material formulation (molar ratio) *2
Inherent
Tm Td
Example
No.
BHB
NDC BPDC
HQDA
DABP
DADE
DABE
REDA
ABA
Viscosity
(°C.)
(°C.)
__________________________________________________________________________
9 B-1
10 10 20 60 2.56 286
416
10 B-2
10 10 20 60 3.07 355
415
11 B-3
10 10 20 60 1.96 269
404
12 B-4
10 10 20 60 0.87 *1
406
13 B-5
10 10 20 60 2.73 *1
407
14 B-6
10 10 20 60 2.27 *1
401
__________________________________________________________________________
Note 1: *1 = Not detectable
Note 2: *2
BHB: 1,6bis(phenoxy)hexane-4,4dicarboxylic acid
NDC: 2,6naphthalenedicarboxylic acid
BPDC: 4,4biphenyldicarboxylic acid
HQDA: hydroquinone diacetate
DABP: 4,4diacetoxybiphenyl
DADE: 4,4diacetoxydiphenyl ether
DABE: 4,4' diacetoxybenzophenone
REDA: resorcinol diacetate
ABA: pacetoxybenzoic acid
Tm: DSCmeasured temperature indicating endoterm caused by melting of a
polymer
Td: Starting temperature of thermal decompositon
TABLE 3
______________________________________
Calculated Found
Polyester No.
C (%) H (%) O (%) C (%) H (%) O (%)
______________________________________
A-1 70.96 4.33 24.71 70.53 4.13 25.34
A-2 73.05 4.17 22.78 73.02 4.12 22.86
A-3 71.57 4.09 24.34 71.28 4.10 24.62
A-4 72.00 4.03 23.98 71.54 4.07 24.39
A-5 70.69 4.05 25.26 69.88 4.02 26.10
A-6 72.22 4.05 23.73 71.22 3.96 24.82
A-7 74.31 4.17 21.52 74.93 4.21 20.85
A-8 72.89 4.09 23.03 73.45 4.20 22.35
B-1 71.56 4.05 24.39 71.35 3.93 24.72
B-2 71.93 4.12 23.95 71.87 4.12 24.01
B-3 74.07 4.23 21.71 73.55 4.27 22.18
B-4 72.63 4.15 23.22 72.52 4.08 23.40
B-5 73.03 4.09 22.89 73.07 3.98 22.95
B-6 71.93 4.12 23.95 72.43 4.00 23.57
______________________________________
TABLE 4
______________________________________
Measurement Load Melt-viscosity
Polyester No.
temperature (°C.)
(kg) (poise)
______________________________________
A-1 350 50 167,000
A-2 330 10 7,760
A-3 350 10 24,700
A-4 300 10 3,870
A-5 350 10 9,390
A-6 280 10 6,840
A-7 280 10 286
A-8 280 10 42,500
B-1 280 10 1,310
B-2 350 50 434
B-3 280 10 223
B-4 350 50 183,000
B-5 350 50 440
B-6 350 50 142,500
______________________________________
Claims (6)
1. A melt-processable copolyester comprising:
a recurring structural unit (I) of the following formula (1), ##STR9## a recurring structural unit (II) of the following formula (2),
--OC--X--CO-- (2)
wherein X is at least one member selected from the group consisting of ##STR10## a recurring structural unit (III) of the following formula (3)
--O--Y--O-- (3)
wherein Y is at least one member selected from the group consisting of ##STR11## a recurring structural unit (IV) of the following formula (4)
--O--Z--CO-- (4)
wherein Z represents at least one member selected from the group consisting of ##STR12## the ratio of the recurring structural unit (III) to the recurring structural units [(I)+(II)+(III)+(IV)] in total being 5 to 80 mole % the recurring structural units [(I)+(II)] being substantially equimolar to the recurring structural unit (III), the ratio of the recurring structural unit (I) to the recurring structural units [(I)+(II)] in total being 10 to 90 mole %, and the copolyester having an inherent viscosity (ln ηrel)/C, measured in a concentration of 0.16g/dl in pentafluorophenol at 60° C., of not less than 0.3 dl/g.
2. A copolyester according to claim 1 which has an inherent viscosity in the range of from 0.5 to 8.0.
3. A copolyester according to claim 1 wherein the ratio of the structural unit (IV) to the structural units [(I)+(II)+(III)+(IV)] in total is 40 to 70 mole %.
4. A copolyester according to claim 1 wherein the ratio of the structural unit (I) to the structural units [(I)+(II)] is 15 to 85 mole %.
5. A copolyester according to claim 1 wherein X in the formula (2) for the structural unit (II) is ##STR13## and Y in the formula (3) for the structural unit (III) and Z in the formula (4) for the structural unit (IV) each represent ##STR14##
6. A copolyester according to claim 1 wherein X in the formula (2) for the structural unit (II) is ##STR15## Y in the formula (3) for the structural unit (III) is at least one member selected from the group consisting of ##STR16## and Z in the formula (4) for the structural unit (IV) is ##STR17##
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP1027478A JPH02208317A (en) | 1989-02-08 | 1989-02-08 | Copolyester |
| JP1-27478 | 1989-02-08 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US4983707A true US4983707A (en) | 1991-01-08 |
Family
ID=12222229
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/473,153 Expired - Fee Related US4983707A (en) | 1989-02-08 | 1990-01-31 | Copolyester from 1,6-bis(phenoxy)hexane-4,4'-dicarboxylate |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US4983707A (en) |
| EP (1) | EP0382438A3 (en) |
| JP (1) | JPH02208317A (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5399428A (en) * | 1994-03-11 | 1995-03-21 | Monsanto Company | Flame retardant polyester copolymers |
| US5399429A (en) * | 1994-03-11 | 1995-03-21 | Monsanto Company | Flame retardant recycled polyester copolymers |
| US5703134A (en) * | 1994-03-11 | 1997-12-30 | Monsanto Company | Copolymers of recycled polyester |
| US5847070A (en) * | 1993-02-18 | 1998-12-08 | Monsanto Company | Hydroxy ethyl bibenzoate |
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| US3778410A (en) * | 1972-09-28 | 1973-12-11 | Eastman Kodak Co | Process for preparing a final copolyester by reacting a starting polyester with an acyloxy aromatic carboxylic acid |
| US4161470A (en) * | 1977-10-20 | 1979-07-17 | Celanese Corporation | Polyester of 6-hydroxy-2-naphthoic acid and para-hydroxy benzoic acid capable of readily undergoing melt processing |
| US4605727A (en) * | 1984-03-09 | 1986-08-12 | Director General Of The Agency Of Industrial Science And Technology | High modulus polyester |
| US4663422A (en) * | 1984-10-30 | 1987-05-05 | Director General Of The Agency Of Industrial Science And Technology | Aromatic polyesters and their shaped articles |
| US4906724A (en) * | 1988-04-11 | 1990-03-06 | Japan as represented by the Director General of Agency of Industrial Science and Technology | High modulus polyester from 4,4'-diphenyldicarboxylic acid |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4238598A (en) * | 1979-02-08 | 1980-12-09 | Fiber Industries, Inc. | Polyester of para-hydroxy benzoic acid, 1,2-bis(para-carboxy phenoxy)ethane, terephthalic acid and hydroquinone capable of forming an anisotropic melt which readily undergoes melt processing |
| JPS57138919A (en) * | 1981-02-23 | 1982-08-27 | Asahi Chem Ind Co Ltd | Fiber or film formed from polyester type polymer presenting flow birefringence |
| EP0305070B1 (en) * | 1987-08-11 | 1993-03-03 | Mitsubishi Gas Chemical Company, Inc. | A melt-processable copolyester |
| JP2590483B2 (en) * | 1987-08-11 | 1997-03-12 | 三菱瓦斯化学株式会社 | Copolyester |
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1989
- 1989-02-08 JP JP1027478A patent/JPH02208317A/en active Pending
-
1990
- 1990-01-31 US US07/473,153 patent/US4983707A/en not_active Expired - Fee Related
- 1990-02-05 EP EP19900301159 patent/EP0382438A3/en not_active Withdrawn
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| US3778410A (en) * | 1972-09-28 | 1973-12-11 | Eastman Kodak Co | Process for preparing a final copolyester by reacting a starting polyester with an acyloxy aromatic carboxylic acid |
| US4161470A (en) * | 1977-10-20 | 1979-07-17 | Celanese Corporation | Polyester of 6-hydroxy-2-naphthoic acid and para-hydroxy benzoic acid capable of readily undergoing melt processing |
| US4605727A (en) * | 1984-03-09 | 1986-08-12 | Director General Of The Agency Of Industrial Science And Technology | High modulus polyester |
| US4663422A (en) * | 1984-10-30 | 1987-05-05 | Director General Of The Agency Of Industrial Science And Technology | Aromatic polyesters and their shaped articles |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5847070A (en) * | 1993-02-18 | 1998-12-08 | Monsanto Company | Hydroxy ethyl bibenzoate |
| US5399428A (en) * | 1994-03-11 | 1995-03-21 | Monsanto Company | Flame retardant polyester copolymers |
| US5399429A (en) * | 1994-03-11 | 1995-03-21 | Monsanto Company | Flame retardant recycled polyester copolymers |
| US5703134A (en) * | 1994-03-11 | 1997-12-30 | Monsanto Company | Copolymers of recycled polyester |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH02208317A (en) | 1990-08-17 |
| EP0382438A2 (en) | 1990-08-16 |
| EP0382438A3 (en) | 1992-01-15 |
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